Exceptional Fill/Finish Flexibility — The Right Scale At The Right Time

As drug sponsors aim to bring more innovative, complex therapeutics to market, the demand for sterile injectable development and cGMP fill/finish manufacturing is increasing. However, sterile liquid & lyophilized dosage forms require specialized equipment and practices to ensure patient safety and product efficacy.

Leveraging a CDMO's expertise and facilities to support high-speed filling for vials and bottles, prefilled syringes, and flexible IV bags can help meet project milestones on time and deliver treatments to patients in need. August Bioservices' formulation development, cGMP laboratories, and cGMP manufacturing capabilities, as well as the team of experts on-site, will support your molecule's journey from preclinical through commercialization.